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Prognostic Score and Cytogenetic Risk Classification for Chronic Lymphocytic Leukemia Patients: Center for International Blood and Marrow Transplant Research Report.
Kim, Haesook T; Ahn, Kwang Woo; Hu, Zhen-Huan; Davids, Matthew S; Volpe, Virginia O; Antin, Joseph H; Sorror, Mohamed L; Shadman, Mazyar; Press, Oliver; Pidala, Joseph; Hogan, William; Negrin, Robert; Devine, Steven; Uberti, Joseph; Agura, Edward; Nash, Richard; Mehta, Jayesh; McGuirk, Joseph; Forman, Stephen; Langston, Amelia; Giralt, Sergio A; Perales, Miguel-Angel; Battiwalla, Minoo; Hale, Gregory A; Gale, Robert Peter; Marks, David I; Hamadani, Mehdi; Ganguly, Sid; Bacher, Ulrike; Lazarus, Hillard; Reshef, Ran; Hildebrandt, Gerhard C; Inamoto, Yoshihiro; Cahn, Jean-Yves; Solh, Melhem; Kharfan-Dabaja, Mohamed A; Ghosh, Nilanjan; Saad, Ayman; Aljurf, Mahmoud; Schouten, Harry C; Hill, Brian T; Pawarode, Attaphol; Kindwall-Keller, Tamila; Saba, Nakhle; Copelan, Edward A; Nathan, Sunita; Beitinjaneh, Amer; Savani, Bipin N; Cerny, Jan; Grunwald, Michael R.
Afiliação
  • Kim HT; Department of Data Sciences, Dana-Farber Cancer Institute, Boston, Massachusetts, and Harvard School of Public Health, Boston, Massachusetts. htkimc@jimmy.harvard.edu wsaber@mcw.edu.
  • Ahn KW; Division of Biostatistics, Institute for Health and Society, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Hu ZH; CIBMTR (Center for International Blood and Marrow Transplant Research), Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Davids MS; CIBMTR (Center for International Blood and Marrow Transplant Research), Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Volpe VO; Division of Hematologic Malignancies, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Antin JH; Department of Internal Medicine, Division of Oncology's Neag Cancer Center, University of Connecticut Health Center, Farmington, Connecticut.
  • Sorror ML; Division of Hematologic Malignancies, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Shadman M; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Press O; Division of Medical Oncology, Department of Medicine, University of Washington School of Medicine, Seattle, Washington.
  • Pidala J; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Hogan W; Division of Medical Oncology, Department of Medicine, University of Washington School of Medicine, Seattle, Washington.
  • Negrin R; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Devine S; Department of Blood and Marrow Transplantation, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
  • Uberti J; Departments of Hematology and Transplant Center, Mayo Clinic Rochester, Rochester, Minnesota.
  • Agura E; Stanford Health Care, Stanford, California.
  • Nash R; CIBMTR (Center for International Blood and Marrow Transplant Research), National Marrow Donor Program/Be the Match, Minneapolis, Minnesota.
  • Mehta J; Karmanos Cancer Institute, Detroit, Michigan.
  • McGuirk J; Baylor University Medical Center, Dallas, Texas.
  • Forman S; Colorado Blood Institute, Denver, Colorado.
  • Langston A; Northwestern medicine, Chicago, Illinois.
  • Giralt SA; University of Kansas, Westood, Kansas.
  • Perales MA; City of Hope Medical Center, Duarte, California.
  • Battiwalla M; Department of Hematology and Medical Oncology, Winship Cancer Institute of Emory University, Atlanta, Georgia.
  • Hale GA; Adult Bone Marrow Transplantation Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Gale RP; Adult Bone Marrow Transplantation Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Marks DI; Hematology Branch, Sarah Cannon BMT Program, Nashville, Tennessee.
  • Hamadani M; Department of Hematology/Oncology, Johns Hopkins All Children's Hospital, St. Petersburg, Florida.
  • Ganguly S; Hematology Research Centre, Division of Experimental Medicine, Department of Medicine, Imperial College London, London, United Kingdom.
  • Bacher U; Adult Bone Marrow Transplant, University Hospitals Bristol NHS Trust, Bristol, United Kingdom.
  • Lazarus H; Division of Biostatistics, Institute for Health and Society, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Reshef R; Division of Hematological Malignancy and Cellular Therapeutics, University of Kansas Health System, Kansas City, Kansas.
  • Hildebrandt GC; Department of Hematology, Inselspital, Bern University Hospital, Bern, Switzerland.
  • Inamoto Y; Interdisciplinary Clinic for Stem Cell Transplantation, University Cancer Center Hamburg, Hamburg, Germany.
  • Cahn JY; Seidman Cancer Center, University Hospitals Cleveland Medical Center, Case Western Reserve University, Cleveland, Ohio.
  • Solh M; Blood and Marrow Transplantation Program and Columbia Center for Translational Immunology, Columbia University Medical Center, New York, New York.
  • Kharfan-Dabaja MA; Markey Cancer Center, University of Kentucky, Lexington, Kentucky.
  • Ghosh N; Division of Hematopoietic Stem Cell Transplantation, National Cancer Center Hospital, Tokyo, Japan.
  • Saad A; Department of Hematology, CHU Grenoble Alpes, Grenoble, France.
  • Aljurf M; The Blood and Marrow Transplant Group of Georgia, Northside Hospital, Atlanta, Georgia.
  • Schouten HC; Division of Hematology-Oncology, Blood and Marrow Transplantation Program, Mayo Clinic, Jacksonville, Florida.
  • Hill BT; Department of Hematologic Oncology and Blood Disorders, Levine Cancer Institute, Carolinas Healthcare System, Charlotte, North Carolina.
  • Pawarode A; Division of Hematology/Oncology, Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama.
  • Kindwall-Keller T; Department of Oncology, King Faisal Specialist Hospital Center & Research, Riyadh, Saudi Arabia.
  • Saba N; Department of Hematology, Academische Ziekenhuis, Maastricht, the Netherlands.
  • Copelan EA; Department of Hematology and Medical Oncology, Cleveland Clinic Taussig Cancer Institute, Cleveland, Ohio.
  • Nathan S; Blood and Marrow Transplantation Program, Division of Hematology/Oncology, Department of Internal Medicine, The University of Michigan Medical School, Ann Arbor, Michigan.
  • Beitinjaneh A; Division of Hematology/Oncology, University of Virginia Health System, Charlottesville, Virginia.
  • Savani BN; Tulane University Medical Center, New Orleans, Louisiana.
  • Cerny J; Department of Hematologic Oncology and Blood Disorders, Levine Cancer Institute, Carolinas HealthCare System, Charlotte, North Carolina.
  • Grunwald MR; Rush University Medical Center, Chicago, Illinois.
Clin Cancer Res ; 25(16): 5143-5155, 2019 08 15.
Article em En | MEDLINE | ID: mdl-31253630
ABSTRACT

PURPOSE:

To develop a prognostic model and cytogenetic risk classification for previously treated patients with chronic lymphocytic leukemia (CLL) undergoing reduced intensity conditioning (RIC) allogeneic hematopoietic cell transplantation (HCT). EXPERIMENTAL

DESIGN:

We performed a retrospective analysis of outcomes of 606 patients with CLL who underwent RIC allogeneic HCT between 2008 and 2014 reported to the Center for International Blood and Marrow Transplant Research.

RESULTS:

On the basis of multivariable models, disease status, comorbidity index, lymphocyte count, and white blood cell count at HCT were selected for the development of prognostic model. Using the prognostic score, we stratified patients into low-, intermediate-, high-, and very-high-risk [4-year progression-free survival (PFS) 58%, 42%, 33%, and 25%, respectively, P < 0.0001; 4-year overall survival (OS) 70%, 57%, 54%, and 38%, respectively, P < 0.0001]. We also evaluated karyotypic abnormalities together with del(17p) and found that del(17p) or ≥5 abnormalities showed inferior PFS. Using a multivariable model, we classified cytogenetic risk into low, intermediate, and high (P < 0.0001). When the prognostic score and cytogenetic risk were combined, patients with low prognostic score and low cytogenetic risk had prolonged PFS (61% at 4 years) and OS (75% at 4 years).

CONCLUSIONS:

In this large cohort of patients with previously treated CLL who underwent RIC HCT, we developed a robust prognostic scoring system of HCT outcomes and a novel cytogenetic-based risk stratification system. These prognostic models can be used for counseling patients, comparing data across studies, and providing a benchmark for future interventions. For future study, we will further validate these models for patients receiving targeted therapies prior to HCT.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia Linfocítica Crônica de Células B / Aberrações Cromossômicas Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia Linfocítica Crônica de Células B / Aberrações Cromossômicas Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article